Disease: Abnormal color vision ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2723341
rs2723341
Entrez Id: 10002
Gene Symbol: NR2E3
NR2E3
CUI: C0234629
Disease:
Abnormal color vision 		C 0.700 CausalMutation CLINVAR